首页> 美国卫生研究院文献>Journal of Clinical Microbiology >Interpretive criteria and quality control parameters for testing of susceptibilities of Haemophilus influenzae and Streptococcus pneumoniae to trimethoprim and trimethoprim-sulfamethoxazole. The Antimicrobial Susceptibility Testing OC Group.
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Interpretive criteria and quality control parameters for testing of susceptibilities of Haemophilus influenzae and Streptococcus pneumoniae to trimethoprim and trimethoprim-sulfamethoxazole. The Antimicrobial Susceptibility Testing OC Group.

机译:测试流感嗜血杆菌和肺炎链球菌对甲氧苄啶和甲氧苄啶-磺胺甲恶唑敏感性的解释性标准和质量控制参数。抗菌药物敏感性试验OC组。

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摘要

Two hundred twenty-eight strains of Haemophilus influenzae and 234 strains of Streptococcus pneumoniae were tested by broth microdilution and disk diffusion methods for susceptibility to trimethoprim (TMP) and TMP-sulfamethoxazole (SMX) to evaluate proposed criteria. Data are presented to support the proposed TMP MIC breakpoints of < or = 2.0 micrograms/ml for susceptibility and > or = 4.0 micrograms/ml for resistance for both species and TMP-SMX MIC breakpoints of < or = 2.0-38 micrograms/ml for susceptibility and > or = 4.0-76 micrograms/ml for resistance. Corresponding zone diameter breakpoints for H. influenzae for both drugs are proposed: < or = 10 mm = resistant; > or = 16 mm = susceptible. A 10-laboratory study documented reproducibility of such tests with standard control strains. The following control limits are proposed for tests of H. influenzae ATCC 49247 against TMP; MIC, 0.12 to 0.5 microgram/ml; zone diameter, 27 to 33 mm. The current limits for TMP-SMX were confirmed. For tests of S. pneumoniae ATCC 49619, MICs of TMP were 1.0 to 4.0 micrograms/ml and the current TMP-SMX MIC range was confirmed. Disk susceptibility tests of either drug against pneumococci were not reproducible, and consequently neither quality control limits nor interpretive criteria could be established. Endpoint interpretation and lot-to-lot variability in Mueller-Hinton agars were significant factors leading to interlaboratory variability.
机译:通过肉汤微量稀释和圆盘扩散法测试了228株流感嗜血杆菌和234株肺炎链球菌对甲氧苄氨嘧啶(TMP)和TMP-磺胺甲恶唑(SMX)的敏感性,以评估拟议标准。所提供的数据可支持拟议的TMP MIC敏感性点≤2.0微克/ ml,对于物种的抗药性>≥4.0微克/ ml,TMP-SMX MIC耐受性≤2.0-38微克/ ml药敏,抗药性≥4.0-76微克/ ml。两种药物的流感嗜血杆菌的相应区域直径断点均建议:<或= 10 mm =耐药; >或= 16毫米=易感。一项10个实验室的研究记录了这种测试方法与标准对照菌株的可重复性。建议对流感嗜血杆菌ATCC 49247进行TMP检测时应遵循以下控制限值; MIC,0.12至0.5微克/毫升;区域直径为27至33毫米。确认了TMP-SMX的当前限制。对于肺炎链球菌ATCC 49619的测试,TMP的MIC为1.0到4.0微克/毫升,并且确定了当前的TMP-SMX MIC范围。两种药物对肺炎球菌的药敏试验均不可重复,因此无法建立质量控制限度或解释性标准。 Mueller-Hinton琼脂的终点解释和批次间变异性是导致实验室间变异性的重要因素。

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